Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g46140 | A01 | 30754929 | C | T | missense_variant | MODERATE | c.169G>A|p.Val57Met |
S32 |
2 | BAA01g46140 | A01 | 30757806 | C | T | upstream_gene_variant | MODIFIER | c.-2709G>A| |
S239 |
3 | BAA01g46140 | A01 | 30757902 | G | A | upstream_gene_variant | MODIFIER | c.-2805C>T| |
S295 |
4 | BAA01g46140 | A01 | 30758043 | G | A | upstream_gene_variant | MODIFIER | c.-2946C>T| |
S276 |
5 | BAA01g46140 | A01 | 30758668 | G | A | upstream_gene_variant | MODIFIER | c.-3571C>T| |
S115 |
6 | BAA01g46140 | A01 | 30759163 | C | T | upstream_gene_variant | MODIFIER | c.-4066G>A| |
S8 |
7 | BAA01g46140 | A01 | 30759319 | G | A | upstream_gene_variant | MODIFIER | c.-4222C>T| |
S244 |
8 | BAA01g46140 | A01 | 30759338 | C | T | upstream_gene_variant | MODIFIER | c.-4241G>A| |
S79 S91 |
9 | BAA01g46140 | A01 | 30759496 | C | T | upstream_gene_variant | MODIFIER | c.-4399G>A| |
S153 |
10 | BAA01g46140 | A01 | 30759507 | C | T | upstream_gene_variant | MODIFIER | c.-4410G>A| |
S146 |
11 | BAA01g46140 | A01 | 30759859 | C | T | upstream_gene_variant | MODIFIER | c.-4762G>A| |
S305 |